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Pharmacokinetics of Maxmarvil® in Healthy Postmenopausal Women (YY_PK_2011)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified February 2012 by Yuyu Pharma, Inc..
Recruitment status was:  Recruiting
Information provided by (Responsible Party):
Yuyu Pharma, Inc. Identifier:
First received: February 1, 2012
Last updated: February 13, 2012
Last verified: February 2012
This study will evaluate clinical safety and pharmacokinetics of Maxmarvil® in healthy postmenopausal women

Condition Intervention Phase
Drug: Maxmarvil®
Phase 1

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Pharmacokinetics of a Single Oral Dose of Maxmarvil® in Healthy Postmenopausal Women Without a Previous History of Fractures

Resource links provided by NLM:

Further study details as provided by Yuyu Pharma, Inc.:

Primary Outcome Measures:
  • analysis of Alendronate concentrate [ Time Frame: pre-dose, post dose 0-6hour, 6-12hour, 12-24hour ]
    If the CrCL value is less than 75%, it is considered that collected urine is not appropriate and collected urine is exclusived for analysis of pharmacokinetics

Estimated Enrollment: 20
Study Start Date: October 2011
Estimated Study Completion Date: September 2012
Estimated Primary Completion Date: July 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
No Intervention: Maxmarvil®
single-arm study
Drug: Maxmarvil®
Drug : Maxmarvil® 1tablet one time in clinical trial, PO medication
Other Name: Alendronate 5mg + calcitriol 0.5 μg

Detailed Description:

Pharmacokinetics of a single Oral Dose of Maxmarvil® in healthy postmenopausal women without a previous history of fractures

  1. evaluation of Pharmacokinetics

    • Urine collection : Pre-dose(pre 1hour), post-dose 0~6 hour, 6~12 hour, 12~24 hour
    • Evaluation Variables : Aet
  2. Evaluation of safety, pharmacodynamics

    • Adverse Event : check it every and frequently
    • Physical exam : screening, just before injection, post-dose 24 hour and post-study visit
    • Vital sign : screening, just before injection, post-dose 1 hour, 24 hour and post-study visit
    • Laboratory test : screening, post-dose 24hour

Ages Eligible for Study:   55 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Screening test in healthy postmenopausal women without a previous history of fracture
  • Normal range in laboratory test arranged by principal investigator because of the character of medicine
  • over 50kg, body weight is in ± 20% of ideal body weight Written concent by himself and following the protocol after understanding of the explained clinical trial

Exclusion Criteria:

  • Subject who have taken something to induce and inhibit the drug metabolizing enzyme within 1 month like Barbiturate.
  • Subject who have a history of drug abuse and got a positive in urine test for drug abuse.
  • Subject who have taken a prescription only medicine or an oriental medicine within 2 weeks after first administration the clinical drug trial , taken a OTC within 1 week after first administration the clinical drug trial like some OTC including calcium, an antacids, multiple vitamin, mineral.
  • Subject who have been chronic drinking(over 21 units/week) or can not stop drinking during the clinical trial.
  • Subject who have smoked over 10 unit/day for 3months.
  • Subject who have light or clear hypersensitivity reaction about OTC(aspirin, antibiotic medication) or bisphosphonates(alendronate)
  • Subject who have got a disease about liver, kidney, neurology, respiratory, endocrine, hematooncology, cardiovascular, musculoskeletal, psychological or history of fracture within 12months or a tooth extraction within 6month
  • Subject who have a history of gastrointestinal disease or stomach surgery without appendectomy, herniotomy having an effort the absorb of clinical drug trial.
  • Subject who have a esophageal disease like esophagitis, esophageal ulcer, esophagus erosion, esophagorrhaphy, esophagostenosis, dysphagia.
  • Subject who can not keep the sitting position for 30minutes
  • Subject who is out of normal range of calcium concentration in blood (8.8 ~ 10.5 mg/dl)
  • Subject who is hypotension(systolic blood pressure ≤ 90mmHg or diastolic blood pressure ≤ 50 mmHg ) or hypertension(systolic blood pressure ≥ 150mmHg or diastolic blood pressure ≥ 100 mmHg ) in sitting position after rest 3 minutes
  • join the other clinical trial within 2months after administration of the clinical drug trial.
  • Subject who have donated whole blood within 2 months or plasma within 1 month.
  • Subject who have a grapefruit and something including caffeine in close season(from 3 days before administration to discharge from the hospital )
  • For the result of laboratory and the other reason subject is considered unsuitable by principal's decision
  Contacts and Locations
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Please refer to this study by its identifier: NCT01526278

Contact: yoon-suk chung, MD,Ph.D 82-31-219-5127
Contact: kyeongsuk seo, BS 82-2-2253-6600

Korea, Republic of
Ajou University Hospital Recruiting
Suwon, Korea, Republic of
Contact: Yoon-suk Chung, MD,PhD    82-31-219-5127   
Contact: Min-suk Lee, MD    82-31-5162-2751   
Sponsors and Collaborators
Yuyu Pharma, Inc.
Principal Investigator: yoon-suk chung, MD,PhD Ajou university hospotal
  More Information

Responsible Party: Yuyu Pharma, Inc. Identifier: NCT01526278     History of Changes
Other Study ID Numbers: YY_PK_2011
Study First Received: February 1, 2012
Last Updated: February 13, 2012

Keywords provided by Yuyu Pharma, Inc.:

Additional relevant MeSH terms:
Bone Diseases, Metabolic
Bone Diseases
Musculoskeletal Diseases
Bone Density Conservation Agents
Physiological Effects of Drugs processed this record on April 27, 2017